C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias

Karla P. Figueroa; Shi Rui Gan; Susan Perlman; George Wilmot; Christopher M. Gomez; Jeremy Schmahmann; Henry Paulson; Vikram G. Shakkottai; Sarah H. Ying; Theresa Zesiewicz; Khalaf Bushara; Michael Geschwind; Guangbin Xia; S. H. Subramony; Tetsuo Ashizawa; Stefan M. Pulst; Sheng Han Kuo

doi:10.1002/mds.27258

C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias

Karla P. Figueroa, Shi Rui Gan, Susan Perlman, George Wilmot, Christopher M. Gomez, Jeremy Schmahmann, Henry Paulson, Vikram G. Shakkottai, Sarah H. Ying, Theresa Zesiewicz, Khalaf Bushara, Michael Geschwind, Guangbin Xia, S. H. Subramony, Tetsuo Ashizawa, Stefan M. Pulst, Sheng Han Kuo

Research output: Contribution to journal › Letter › peer-review

2 Scopus citations

Original language	English (US)
Pages (from-to)	497-498
Number of pages	2
Journal	Movement Disorders
Volume	33
Issue number	3
DOIs	https://doi.org/10.1002/mds.27258
State	Published - Mar 2018
Externally published	Yes

ASJC Scopus subject areas

Neurology
Clinical Neurology

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10.1002/mds.27258

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Figueroa, K. P., Gan, S. R., Perlman, S., Wilmot, G., Gomez, C. M., Schmahmann, J., Paulson, H., Shakkottai, V. G., Ying, S. H., Zesiewicz, T., Bushara, K., Geschwind, M., Xia, G., Subramony, S. H., Ashizawa, T., Pulst, S. M., & Kuo, S. H. (2018). C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias. Movement Disorders, 33(3), 497-498. https://doi.org/10.1002/mds.27258

C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias. / Figueroa, Karla P.; Gan, Shi Rui; Perlman, Susan; Wilmot, George; Gomez, Christopher M.; Schmahmann, Jeremy; Paulson, Henry; Shakkottai, Vikram G.; Ying, Sarah H.; Zesiewicz, Theresa; Bushara, Khalaf; Geschwind, Michael; Xia, Guangbin; Subramony, S. H.; Ashizawa, Tetsuo; Pulst, Stefan M.; Kuo, Sheng Han.

In: Movement Disorders, Vol. 33, No. 3, 03.2018, p. 497-498.

Research output: Contribution to journal › Letter › peer-review

Figueroa, KP, Gan, SR, Perlman, S, Wilmot, G, Gomez, CM, Schmahmann, J, Paulson, H, Shakkottai, VG, Ying, SH, Zesiewicz, T, Bushara, K, Geschwind, M, Xia, G, Subramony, SH, Ashizawa, T, Pulst, SM & Kuo, SH 2018, 'C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias', Movement Disorders, vol. 33, no. 3, pp. 497-498. https://doi.org/10.1002/mds.27258

Figueroa, Karla P. ; Gan, Shi Rui ; Perlman, Susan ; Wilmot, George ; Gomez, Christopher M. ; Schmahmann, Jeremy ; Paulson, Henry ; Shakkottai, Vikram G. ; Ying, Sarah H. ; Zesiewicz, Theresa ; Bushara, Khalaf ; Geschwind, Michael ; Xia, Guangbin ; Subramony, S. H. ; Ashizawa, Tetsuo ; Pulst, Stefan M. ; Kuo, Sheng Han. / C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias. In: Movement Disorders. 2018 ; Vol. 33, No. 3. pp. 497-498.

@article{76de4bf5e8c948caa8fa1fd08e9505d1,

title = "C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias",

author = "Figueroa, {Karla P.} and Gan, {Shi Rui} and Susan Perlman and George Wilmot and Gomez, {Christopher M.} and Jeremy Schmahmann and Henry Paulson and Shakkottai, {Vikram G.} and Ying, {Sarah H.} and Theresa Zesiewicz and Khalaf Bushara and Michael Geschwind and Guangbin Xia and Subramony, {S. H.} and Tetsuo Ashizawa and Pulst, {Stefan M.} and Kuo, {Sheng Han}",

note = "Funding Information: Funding agencies: The Clinical Research Consortium-Spinocerebellar Ataxia (CRC-SCA) natural history study is supported by the Rare Disease Clinical Research Network (RC1NS068897), and the National Ataxia Foundation. Dr. Stefan Pulst is supported by NIH/National Institute of Neurological Disorders and Stroke (NINDS) RC4NS073009, R01NS033123, R37NS033123. Dr. Kuo is supported by the NINDS K08 NS083738, Louis V. Gerstner Jr. Scholarship, American Brain Research Training Fellowship, Parkinson Disease Foundation, American Parkinson{\textquoteright}s Disease Association, Rare Disease Clinical Research Network (RC1NS068897), International Essential Tremor Foundation, and National Institute of Environmental Health Sciences (NIEHS) pilot grant ES009089, the Smart Foundation. Dr. Gan is supported by the National Natural Science Foundation of China (U1505222).",

year = "2018",

month = mar,

doi = "10.1002/mds.27258",

language = "English (US)",

volume = "33",

pages = "497--498",

journal = "Movement Disorders",

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T1 - C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias

AU - Figueroa, Karla P.

AU - Gan, Shi Rui

AU - Perlman, Susan

AU - Wilmot, George

AU - Gomez, Christopher M.

AU - Schmahmann, Jeremy

AU - Paulson, Henry

AU - Shakkottai, Vikram G.

AU - Ying, Sarah H.

AU - Zesiewicz, Theresa

AU - Bushara, Khalaf

AU - Geschwind, Michael

AU - Xia, Guangbin

AU - Subramony, S. H.

AU - Ashizawa, Tetsuo

AU - Pulst, Stefan M.

AU - Kuo, Sheng Han

N1 - Funding Information: Funding agencies: The Clinical Research Consortium-Spinocerebellar Ataxia (CRC-SCA) natural history study is supported by the Rare Disease Clinical Research Network (RC1NS068897), and the National Ataxia Foundation. Dr. Stefan Pulst is supported by NIH/National Institute of Neurological Disorders and Stroke (NINDS) RC4NS073009, R01NS033123, R37NS033123. Dr. Kuo is supported by the NINDS K08 NS083738, Louis V. Gerstner Jr. Scholarship, American Brain Research Training Fellowship, Parkinson Disease Foundation, American Parkinson’s Disease Association, Rare Disease Clinical Research Network (RC1NS068897), International Essential Tremor Foundation, and National Institute of Environmental Health Sciences (NIEHS) pilot grant ES009089, the Smart Foundation. Dr. Gan is supported by the National Natural Science Foundation of China (U1505222).

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DO - 10.1002/mds.27258

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C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias

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